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Rage gene promoter polymorphisms and diabetic retinopathy in a clinic-based population from South India

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dc.contributor.author Ramprasad, S
dc.contributor.author Radha, V
dc.contributor.author Mathias, R A
dc.contributor.author Majumder, P P
dc.contributor.author Rao, M R S
dc.contributor.author Rema, M
dc.date.accessioned 2012-02-10T09:26:31Z
dc.date.available 2012-02-10T09:26:31Z
dc.date.issued 2007-03
dc.identifier 0950-222X en_US
dc.identifier.citation Eye 21(3), 395-401 (2007) en_US
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/10572/377
dc.description Restricted Access en_US
dc.description.abstract Purpose The main objective of this study was to evaluate if the -429T/C, -374T/A and 63 bp deletion polymorphisms in the RAGE gene are associated with diabetic retinopathy (DR) among Type 2 diabetic subjects in a clinic-based population from South India. Methods We screened 149 normal glucose tolerant subjects (NGT), 189 Type 2 diabetes subjects without retinopathy (DM) and 190 subjects with DR for these polymorphisms using the PCR-RFLP method. DR was diagnosed by grading color fundus photography. Logistic regression models were used to evaluate the association of individual polymorphisms with DR. Expectation maximization algorithms were implemented in haplotype tests of association to examine the combined effects of -429T/C and -374T/A polymorphisms on DR. Results The allelic frequencies of -429T are 0.83 in NGT, 0.84 in DM and 0.85 in DR subjects, and that of -374T are 0.93 in NGT, 0.92 in DM and 0.88 in DR subjects. The -374 polymorphism was found to be associated with non-proliferative retinopathy when this subgroup was compared to the DM group (OR 1.814, 95% CI = 1.005-3.273). However, this association was not obvious when both the subphenotypes of DR (the nonproliferative and proliferative DR groups) were studied jointly. We found no evidence for associations between the -429T/C polymorphism and the DR phenotype. Finally, extension to a 2-SNP haplotype did not reveal any significant statistical difference between the groups (P = 0.668). Conclusion In this study, we found a modest association with the -374T/A polymorphism in the nonproliferative DR subgroup. en_US
dc.description.uri http://dx.doi.org/10.1038/sj.eye.6702239 en_US
dc.language.iso en en_US
dc.publisher Nature Publishing Group en_US
dc.rights © 2007 Nature Publishing Group en_US
dc.subject diabetic retinopathy en_US
dc.subject RAGE polymorphism en_US
dc.subject -374 TA en_US
dc.subject -429 TC en_US
dc.subject 63 bp deletion en_US
dc.subject Cultured Endothelial-Cells en_US
dc.subject End-Products Gene en_US
dc.subject Association en_US
dc.subject Nephropathy en_US
dc.subject Receptor en_US
dc.subject Prevalence en_US
dc.subject Microalbuminuria en_US
dc.subject Complications en_US
dc.subject Projections en_US
dc.subject Reductase en_US
dc.title Rage gene promoter polymorphisms and diabetic retinopathy in a clinic-based population from South India en_US
dc.type Article en_US


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